Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694398Generated: October 26, 2026

Pyrrolidine → 1-(4-Bromo-2-fluorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1694398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant4-Bromo-2-fluorobenzyl bromideHCID 2733660—
SolventAcetonitrileHCID 6342—
Product1-(4-Bromo-2-fluorobenzyl)pyrrolidineHCID 2226672390%

Reaction Conditions

Temperature10 °C

Reaction Steps

A 4-L RB flask, equipped a magnetic stirring bar was charged with pyrrolidine (363 g, 426 mL, 5.1 mol) and acetonitrile (2750 mL). The mixture was cooled with an ice bath to 10° C., then solid 4-bromo-2-fluorobenzylbromide (MATRIX, Cat. #: 1707, 375 g, 1.4 mol) was added in 6 portions, keeping temperature below 20° C. The mixture was stirred at RT for 4 h. The solvent was removed under vacuum. Then 2 L of sat. Na2CO3 aq. and 500 mL of water was added, and the mixture was extracted with DCM (3×700 mL). The extract was dried over Na2SO4 and evaporated. The resulting light yellow oil was distilled under vacuum (˜1 mm, bp. 125° C.) to give 324.5 g (90%) of the product as a colorless oil. LCMS (M+H): 258.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158673B2
Source datasetuspto-grants-2012_04
ORD IDord-5d89c8324c174b509384eb152e3c9d57
Source noteuspto-grants-2012_04